GLYAT glycine-N-acyltransferase
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 48 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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50 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
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Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | ACGNAT |
SYNONYM | CAT |
SYNONYM | GAT |
MIM | 607424 OMIM |
HGNC | HGNC:13734 HGNC |
Ensembl | ENSG00000149124 Ensembl |
AllianceGenome | HGNC:13734 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000344743.8 | hg38 | chr11 | 58,708,757 | 58,731,943 | 23,187 |
ENST00000278400.3 | hg38 | chr11 | 58,710,083 | 58,731,974 | 21,892 |
ENST00000611865.4 | hg38 | chr11 | 58,708,758 | 58,724,496 | 15,739 |
ENST00000529732.5 | hg38 | chr11 | 58,709,668 | 58,728,729 | 19,062 |
ENST00000344743.8 | hg19 | chr11 | 58,476,230 | 58,499,416 | 23,187 |
ENST00000611865.4 | hg19 | chr11 | 58,476,231 | 58,491,969 | 15,739 |
ENST00000529732.5 | hg19 | chr11 | 58,477,141 | 58,496,202 | 19,062 |
ENST00000278400.3 | hg19 | chr11 | 58,477,556 | 58,499,447 | 21,892 |
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